Clinical Project Manager

Mansfield, MA

Join an established leader in the medical device diagnostic arena. Great team environment, career growth and compensation package!


  • Independently manage clinical trials
  • Ensure clinical studies are monitored in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines and SOPs, utilizing knowledge of the diagnostic area
  • Assist clinical sites with IRB submission / documentation, if needed
  • Lead cross-functional effort to summarize and present clinical study data
  • Utilize a working knowledge of GCP and SOPs to assure compliance with FDA regulations
  • Work cross-functionally with Regulatory Affairs and Quality Management
  • Develop other team members through mentoring and coaching in complex subjects


  • BS/BA in life science discipline or equivalent combination of education and experience
  • 10+ years of successful experience in related field and successful performance of responsibilities presented above
  • Experience in in vitro diagnostics a plus
  • Strong writing and presentation skills
  • Ability to travel, domestic and international, depending upon project need, periodically up to 30-50% in US; less than 10% internationally

Inquiries and resumes to: Kathy Provost at OR 978/952-6425

For more information, please visit

About the Author
John Compton
John has served as a Medical Device Industry Executive Recruiter, building relationships specifically in New England since 2002. He earned his BS in Mechanical Engineering from the US Military Academy at West Point, NY and is a Babson MBA. John is also a former Army Officer and US Army Ranger School Leadership Award Recipient.